Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_provenance.
- NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_assertion description "[Role of the RUNX2 p.R225Q mutation in cleidocranial dysplasia: a rare presentation and an analysis of the RUNX2 protein structure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_provenance.
- NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_assertion evidence source_evidence_literature NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_provenance.
- NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_assertion SIO_000772 24634175 NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_provenance.
- NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_assertion wasDerivedFrom befree-20150227 NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_provenance.
- NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_assertion wasGeneratedBy ECO_0000203 NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP284554.RAVlDPITt1mB5xl4n4dYWBVpV_0if4wfZ05RDf6YHrVTk130_provenance.